Abstract
The synthesis of a model of the bistramide D tetrahydropyran ring is achieved using a selective cross-metathesis and an intramolecular Michael addition under kinetic control.
Original language | English |
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Pages (from-to) | 2832-2834 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 49 |
Issue number | 17 |
DOIs | |
Publication status | Published - Apr 21 2008 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Keywords
- Cyclisation
- Metathesis
- Michael addition
- Tetrahydropyran